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Impact of novel processing techniques on the functional properties of egg


products and derivatives: A review

Article  in  Journal of Food Process Engineering · December 2020


DOI: 10.1111/jfpe.13568

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Received: 1 June 2020 Revised: 31 August 2020 Accepted: 16 September 2020
DOI: 10.1111/jfpe.13568

REVIEW ARTICLE

Impact of novel processing techniques on the functional


properties of egg products and derivatives: A review

Muhammad Talha Afraz1 | Moazzam Rafiq Khan1 | Ume Roobab2 |


Mohd Adzahan Noranizan | Brijesh K. Tiwari | Muhammad Tayyab Rashid5 |
3 4

Muhammad Inam-ur-Raheem1 | Seyed Mohammad Bagher Hashemi6 |


Rana Muhammad Aadil1

1
National Institute of Food Science and
Technology, University of Agriculture, Abstract
Faisalabad, Pakistan Eggs are an excellent source of quality proteins. Eggs as a whole and its components
2
School of Food Science and Engineering,
(egg white and egg yolk) are employed in a range of food preparations. Thermal
South China University of Technology,
Guangzhou, China processing employed for stabilizing and improving shelf-life of egg components is
3
Department of Food Technology, Faculty of known to have adverse effect on heat-sensitive proteins leading to protein denatur-
Food Science and Technology, Universiti Putra
Malaysia, Serdang, Malaysia ation and aggregation thus, reducing the required functional, technological, and over-
4
Department of Food Biosciences, Teagasc all quality of egg proteins and other constituents. Therefore, the current challenge is
Food Research Centre, Dublin, Ireland
to identify novel processing techniques that not only improve the intrinsic functional
5
School of Food and Biological Engineering,
Jiangsu University, Zhenjiang, P.R. China
properties of eggs or its components, but also improve the quality of the product.
6
Department of Food Science and Technology, This review focuses on the use of technologies such as ultrasound, pulsed electric
Faculty of Agriculture, Fasa University, field, high-pressure processing, radiofrequency, ultraviolet light, microwave, and cold
Fasa, Iran
plasma for egg products. These novel technologies are known for their advantages
Correspondence over thermal treatments especially in protecting the heat sensitive nature and
Muhammad Inam-ur-Raheem and Rana
Muhammad Aadil, National Institute of Food retaining the overall quality of the egg and egg products. Availability of alternatives
Science and Technology, University of processing has significantly improved the structural properties, techno-functional,
Agriculture, Faisalabad, 38000, Pakistan.
Email: raheemuaf@gmail.com (M. I. R.) and nutritional and as well improving the safety egg and egg products.
dilrana89@gmail.com (R. M. A.)
Practical Application
Eggs are consumed worldwide as whole egg or in some cases, consumed partly as
egg whites or egg yolks. Egg components with improved techno-functional proper-
ties can be used in various food industries (such as baking, confectionery, and culi-
nary preparation, etc.). Value addition of new products can be achieved through
modification of egg proteins. Additionally, these techniques also provide microbial
safety and have a reduced impact on nutritional content and overall food quality.

1 | I N T RO DU CT I O N Madni, & Bekhit, 2018; Arshad et al., 2020). Liquid eggs are rich in
nutrients and have a variety of desirable techno-functional attributes
Current consumers demand that food manufacturers switch to a such as foaming, emulsifying, gelling, coloring, and flavoring properties
more cost-effective, nutritionally stable, and environment-friendly (Bi et al., 2020). These functional properties are applied in products
processing technology, as conventional technologies are seen to such as meat loaves, broths, salad dressing, custards, mayonnaise, and
promote concerns in the aspects of quality, safety, and toxicity (Aadil cakes (Kavuşan & Serdaro
glu, 2019). As well-known, eggs are highly
et al., 2018, 2020; Mukhopadhyay & Ukuku, 2018; Roobab, Aadil, perishable and undergoes considerable chemical, physical and

J Food Process Eng. 2020;e13568. wileyonlinelibrary.com/journal/jfpe © 2020 Wiley Periodicals LLC. 1 of 18


https://doi.org/10.1111/jfpe.13568
2 of 18 AFRAZ ET AL.

microbiological changes during long term storage (Yüceer & Silcock, 2019; Liu, Oey, Bremer, Silcock, et al., 2019; Mirmoghtadaie,
Caner, 2018). Currently, pasteurization (64 C/2.5 min) is a widely Shojaee Aliabadi, & Hosseini, 2016; Zhu et al., 2018a). However, there
employed heat treatment (HT) to provide microbial safety and is a need for a comparative and up-to-date systematic review provid-
increase the shelf life of egg products, but at the expense of deterio- ing crucial information for food industry about the various novel tech-
rated functional properties. Moreover, traditional HTs are neither niques focusing on the modification of structure and functional
energy nor time-efficient and damage the delicate protein structure properties of egg products and derivatives.
(Wei, Lau, Reddy, & Subbiah, 2020) therefore a new and innovative Therefore, the objectives of this review are to discuss:
novel approach are needed.
This review work covers seven different novel technologies for 1. the effects of novel processing technologies on egg products and
egg processing. Selection of the technologies are based on the current derivatives.
trends in the industry as well as developments in the research arena. 2. the improvements brought about by these technologies with
The technologies are ultrasound (US; Caner & Yuceer, 2015; Sheng regard to the techno-functional attributes and microbiological
et al., 2018; Stefanovic et al., 2017; Yüceer & Caner, 2020a, 2020b; status.
Zhu, Vanga, Wang, & Raghavan, 2018b), high hydrostatic pressure 3. the potential of increasing the breadth of applications for egg
(HHP; Hoppe, Jung, Patnaik, & Zeece, 2013; Ma, Lozano-Ojalvo, products and derivatives in the food industries through the use of
Chen, Lopez-Fandiño, & Molina, 2015; Naderi, Pouliot, House, & novel processing technologies.
Doyen, 2017; Savadkoohi, Bannikova, Mantri, & Kasapis, 2016;
Shahbaz et al., 2018), pulsed electric field (PEF; Baba et al., 2018; Liu,
Oey, Bremer, Carne, & Silcock, 2017; Liu, Oey, Bremer, Carne, & 2 | T H E I N T E R V E N T I O N OF N O V E L
Silcock, 2019; Liu et al., 2019; Wu, Zhao, Yang, & Chen, 2014), micro- T E C H N I Q U E S FO R T H E A D V A N C E M E N T O F
wave (MW; Li, Sun, Ma, Jin, & Sheng, 2018; Singh et al., 2018; Zhu, C L O S E - T O F RE S H F O O D P RO DU C T S
Vanga, Wang, & Raghavan, 2018a), ultraviolet light (UV; Holck, Liland,
Drømtorp, Carlehö, & McLeod, 2018; Manzocco, Panozzo, & Today wholesome product that meets clean label requirement is
Nicoli, 2012; Mehdizadeh, Minaei, Torshizi, & Mohajerani, 2014), cold trending across the world, however an uphill battle exist to maintain
plasma (CP; Dasan, Yildirim, & Boyaci, 2018; Dobeic et al., 2016; the stability of end products. Innovative food processing techniques
Georgescu, Apostol, & Gherendi, 2017; Wan, Chen, Pankaj, & are therefore required to ensure food product safety and quality
Keener, 2017), and radio frequency (RF; Boreddy, Birla, Froning, (Naderi, House, Pouliot, & Doyen, 2017). Thermal treatment is an effi-
Thippareddi, & Subbiah, 2014; Boreddy, Thippareddi, Froning, & cient means of food preservation because the vast majority of harmful
Subbiah, 2016; Geveke, Bigley, & Brunkhorst, 2017; Yang pathogens are killed near the boiling point of water. Nevertheless,
et al., 2019). Thus, the efficiency and suitability of available novel market demand for fresh-like food has sparked the development of
technologies, for the processing of egg products and derivatives new technologies, to replace well-established conventional thermal
should be compared and examined. processing (Mukhopadhyay & Ukuku, 2018).
Technologies offers a novel approach to modify and customize the Several modern and advanced, novel processing techniques for
functional properties of egg proteins (Li et al., 2018; Sheng et al., 2018). different food commodities including eggs have been developed in
For example, US (Jun et al., 2020; Yüceer & Caner, 2020a), PEF (Liu recent years to enhance quality and shelf life. Techniques such as US,
et al., 2017), HHP (Singh & Ramaswamy, 2014) have been reported to PEF, HHP, and UV have been used to reduce the microbial risk and
improve the functional properties of egg derivatives, subsequently mod- improve sensory, nutritional, and functional properties, moreover,
ify the properties of egg proteins. Zhu et al. (2018a) reported that US these techniques are environment friendly (Holck et al., 2018;
affect the secondary structure of protein which triggers the exposure of Rahaman et al., 2020; Sheng et al., 2018). For specific applications,
inner hydrophobic and sulfhydryl groups, consequently altering the pro- many new processing techniques have already been industrially
tein surface properties (associated with emulsifying and foaming) and implemented, while many others are being further developed but with
causing the subsequent formation of protein aggregates (associated great potential (Mukhopadhyay & Ukuku, 2018).
with protein gelation) (Li et al., 2018). Furthermore, it has been reported
that sulfhydryl groups and disulfide bonds play an important role in the
gelling process concerning protein gelation (Boreddy et al., 2016). These 3 | CURRENT CHALLENGES AND
techniques could also inactivate the microbial population (Baba POTENTIAL FUTURE PERSPECTIVES
et al., 2018; Dasan et al., 2018; Holck et al., 2018; Naderi, Pouliot,
et al., 2017; Shahbaz et al., 2018) while resulting in “secondary” benefi- Foods produced from novel processing technologies need approval
cial outcomes, which are related to the functionality-enhancing effects. from certain regulation bodies for their market circulation and label-
The effect of non-conventional techniques on protein functional ing. According to the EU regulation, the novel foods result from the
properties, and extending its food applications are well documented chemical, biochemical, and biotechnological reactions (via novel
(Higuera-Barraza, Del Toro-Sanchez, Ruiz-Cruz, & Márquez- processing) that needs to be checked for their safety and intended
lu, 2019; Liu, Oey, Bremer, Carne, &
Ríos, 2016; Kavuşan & Serdarog functional claims. Likewise, some countries already have guideline or
AFRAZ ET AL. 3 of 18

regulations to assist industry players in this area, but many countries the challenge is to enhance their functionality, which would result in
are still without any official standards. The development of appropri- the diversified application, attained conventionally either through
ate equipment, particularly to ensure safety requires process parame- coagulation, complexation with other biopolymers or modification of
ter standardization for regulatory approval, will lead a way for molecular weight such as aggregation or proteolysis (Mulcahy,
improved emerging technologies. With regulations in place, industry Mulvihill, & O'Mahony, 2016; O'Sullivan, Murray, Flynn, &
stakeholders could operate with confidence and safety of the Norton, 2016).
consumers.
Most importantly, foods produced through novel technologies
must not be dangerous or misleading labelling and similar accep- 4.1 | Effect of US on egg and egg products
tance between a novel product and conventionally available food
product (Steinhart, 2007). Furthermore, it has been reported by Table 1 summarizes the effect of US on egg and its derivatives. The
Zhu et al. (2018a) that protein unfolding results in the exposure of influence of US on the structural changes of egg white (EW) proteins
inner buried groups and there is a possibility of a potential allergen was evaluated. Different durations (2–20 min) and frequency
being unfolded as a result of novel processing. According to Besler, (20 ± 0.2 kHz) were used to investigate the effect of US on foaming,
Steinhart, and Paschke (2001), the significance of hidden allergen emulsifying properties, and protein solubility of EW proteins and its
present in egg and egg products are significant but egg protein is susceptibility to alcalase hydrolysis. It was reported that US treatment
sensitive to high pressure. Novel processing applied under severe (20 kHz, 34.11 ± 1.46 W for 2–15 min, 25 ± 1 C) decreased the diam-
condition reported to deteriorate the quality of egg products eter of particle size (368.4 ± 10.51 to 68.4 ± 5.22 nm) and increased
including viscosity, color, and protein and lipid oxidation. A 20% the zeta potential (stability indicator) value (−4.68 ± 1.40 to
increase in viscosity as a result of novel processing would render −22.8 ± 1.06 mV) as compared to control sample. Prolonged treat-
the product undesirable by indirectly causing protein coagulation ment of 20 min caused the denaturation of EW proteins, enhanced
and denaturation (Monfort et al., 2012; Monfort, Saldaña, Condón, the aggregation of molecules, decreased the sulfhydryl (SH) group

Raso, & Alvarez, 2012). However, the disadvantage is minimal when contents and increased the particle size. In contrast, a 15 min treat-
compared to a variety of advantages that the novel processing ment showed an increase in solubility, foaming stability and foaming
offers. Novel techniques that are environmentally friendly and capacity of the EW proteins by 18.1, 193.3, and 60.6%, respectively
cost-effective are the key alternatives for the future. Therefore, compared to untreated samples. The emulsifying properties, foaming
more research are required to understand the impact of novel properties, and solubility of EW proteins can be improved by varying
processing on egg products and derivatives. the sonication time (Stefanovic et al., 2017). In another study, US
treatment of 400 W for 1–16 min on avidin and secondary structures
of EW proteins was evaluated. The study showed that β-sheets was
4 | ULTRASOUND (US) significantly increased while α-helices was decreased after 1 min
treatment than control, while observed 45% of avidin was reduced
In the food industry, US is mainly based on the mechanical waves during the treatment durations (0–16 min). The same study also
have a frequency above the human hearing approach (>16 kHz) and observed no significant (p ≤ .05) change in secondary structure that
that the frequency ranges are classified as low and high energy. US showed low processing ability of US with increase in sonication time
can be classified into high-frequency (100 kHz–1 MHz) low-energy (Zhu et al., 2018a).
diagnostic ultrasound and low-frequency (16–100 kHz) high power The impact of US (20 kHz and 20% amplitude, 20 min,
US. High power US is primarily based on the high shear force and tur- 70–85 C) was investigated on the following properties (surface
bulence generated by the cavitation to break covalent bonds in pro- hydrophobicity, denaturation temperature, SH groups concentra-
teins. The frequency typically employed in US applications is limited in tion, bulk viscosity, foaming, and emulsifying properties) of EW pro-
between 20 kHz and 500 MHz ranges. Low-frequency US is used to teins. An increase in surface hydrophobicity and a decrease in
alter physical and chemical properties of food while that of high fre- apparent viscosity was reported to directly affect the foaming
quency is used to acquire information related to physicochemical stability, while retaining the SH content. They observed that the
properties (Xiong et al., 2016; Zhu et al., 2018a). functional properties of EW solutions can be improved using US
Egg proteins are used in an extensive range of formulations due treatment, decreases the foaming capacity and stability with bulk
to their nutritional value and functional properties (Liu, Yang, viscosity and emulsion stability and the rate of aggregate formation
Bhandari, Meng, & Prakash, 2020). These proteins are capable of air (Arzeni et al., 2012).
bubbles and oil droplets stabilization, gel structure formations, and A change in tertiary structure of ovalbumin was reported
viscosity enhancement because of their high functionality (Shen, Fang, by Xiong et al. (2016) as a result of US application (20 kHz,
Gao, & Guo, 2017). These functional properties are a result of the 35–48 W/m2, 40 min). The secondary structure and subunits had no
complex nature of these molecules because of their exclusive amino significant change. US increased the SHa groups and caused partial
acid arrangements (O'Sullivan, Park, Beevers, Greenwood, & unfolding of ovalbumin. The foaming ability and emulsifying activity
Norton, 2017). To increase the commercial value of proteins, one of were increased, and the interface tension was decreased after US
4 of 18 AFRAZ ET AL.

TABLE 1 Effect of US on egg and egg derivatives

Sample Treatment conditions Overall outcomes References


EW 20 kHz, 360 W power for 10 min, 260% increased foaming ability, 4.9-fold Sheng et al. (2018)
25 C to the control
EW protein 400 W power, for 0–16 min β-sheets increased, α-helices declined, Zhu et al. (2018b)
and 45% reduction in avidin
EW protein 0.2 kHz frequency, 40% amplitude, Decreased partial diameter, increased Stefanovic et al. (2017);
time 2–20 min, 25 ± 1 C zeta potential, and prolonged Boreddy et al. (2016)
treatment caused denaturation
EW protein 20 ± 0.2 kHz, 360 W power for Decreased hydrolysis activation energy, Jovanovic et al. (2016)
15 min, at 25 ± 1 C enthalpy, entropy of activation and
enzyme deactivation energy
Ovalbumin Amplitude (0, 60, 90%), for 20 and Increased free sulfhydryl groups, Xiong et al. (2016)
40 min frequency changed tertiary structure, and partial
unfolding of ovalbumin
EW 20 kHz, 20% amplitude 750 W at Decrease in particle size Arzeni, Pérez, and
pH 7, 5–20 min and 0.5 C Pilosof (2015)
Duck egg 60 kHz, 140 W at for 240, 480, Increased the salt and water content, Mai Dang, Le, and
and 720 min increased EW's hardening ratio, NaCl Songsermpong (2014)
diffusivity coefficient increased by
45–46 times
EW solution 35 and 40 kHz frequency, Changed peptide composition, changed Stefanovic et al. (2014)
(functional hydrolysate) 15–16 min at 25 and 55 C hydrolytic pattern, and higher
antioxidant activity
EW protein 20 kHz frequency, 20% amplitude, Increased surface hydrophobicity, Arzeni, Pérez, and
20 min, 70–85 C decrease in viscosity, and aggregate Pilosof (2012)
formation increased
LWE (inoculated with 40 W frequency, at 55 C for 5 min 3.2-log reduction Huang, Mittal, and
Salmonella enteritidis) Griffiths (2006)

(20 kHz, 35–48 W/m2, 40 min) treatment as compared to control properties of EW's without altering its nutritional value (Knezevic-
(untreated). This could be due to the increase in the surface hydro- Jugovic et al., 2012). Pretreatments with US (20 and 40 kHz, 21.3 and
phobicity and decrease of surface net charge in ovalbumin. Moreover, 30.7 W, 25 C) significantly boost the affinity between alkalase and EW
the foaming and emulsifying stability did not significantly change proteins and increase the enzymatic hydrolysis reaction rate constants
which shows the differences among the US treated and untreated (k2) as compared to thermal treatments. Both pretreatments (probe-type
samples. After US (20 kHz, 35–48 W/m2, 40 min) treatment, large sonicator and US water bath cleaning technique) have shown a signifi-
particle formed due to protein aggregation, while the gelation temper- cant positive effect on the thermodynamics of enzymatic hydrolysis
ature of treated samples was higher as compared to control (Xiong compared to the control reaction. The enzymatic hydrolysis of EW pro-
et al., 2016). Therefore, US can be used to alter the functional proper- teins demonstrated better effect than thermal pretreatment whereby
ties of ovalbumin to promote its usage in food industries (Xiong the enthalpy (ΔH) (63.6 and 54.7%), entropy (ΔS) (4.2 and 3.3%), Gibbs
et al., 2016; Yuceer, 2020). free activation energy (ΔG) (32.2 and 27.9%) and activation energy (Ea)
An increase in foaming property of EW can be achieved when US (61.7 and 53.1%) values were decreased (Knezevic-Jugovic et al., 2012).

(20 kHz, 10 min, 25 C temp) at different powers (90–480 W) was Another application of US as a pretreatment step is in the produc-
used. Above 360 W, US treatment attained the highest foaming tion of functional hydrolysates from EW protein. Different parameters
potential (260%) which was 4.9 times the control treatment (Sheng including US treatment (40 kHz, 15–16 min, 25 and 55 C) were
et al., 2018). Moreover, the lower surface tension and viscosity, and applied to the impact on the hydrolysis process. The US pretreatment
the higher solubility of proteins as a result of US treatment suggested followed by alcalase hydrolysis under optimal conditions (40 kHz,
that the protein was easier to add to the gas–liquid interface Besides, 21.3 W, 25 C, 15 min) caused changes in the peptide composition
the increase in free sulfhydryl groups and surface hydrophobicity and hydrolytic pattern. These conditions will result in hydrolysates
showed that the protein adopted a loose structure after US treatment with increase antioxidant activity than conventional heat (75 C for
(Sheng et al., 2018). 15 min) pretreatment (Stefanovic et al., 2014).
Enzymatic hydrolysis of EW proteins is an important biotechnologi- Salted egg, one of the most popular and traditional preserved egg
cal method used to enhance the chemical, physical and functional products, generally made by brining eggs in saturated salt or by
AFRAZ ET AL. 5 of 18

coating an egg with a soil wrapped mixed with salt for about 5.1 | Effect of HHP on egg and egg products
15–30 days. For instance, the US treatment (60 kHz and 140 W) sig-
nificantly increase the salt and water content of the duck egg during The effect of HHP treatment (100–500 MPa, 10 min, 25 ± 2 C) on
pickling especially under process conditions (240, 480, and 720 min) some functional and physicochemical properties of EY are well
which will led to a faster increase in the salt content of EY and EW reported (Table 2). A significant (p < .05) increase in the viscosity and
(Mai Dang et al., 2014). They observed more rapid increase in the EY's a gradual decline in protein solubility were reported by Yan
hardening ratio during pickling under US (720 min running time). Addi- et al. (2010), after the HHP treatment and these changes could be
tionally, the US could increase the NaCl diffusivity coefficient through due to the aggregation of protein. A gradual decrease in SH contents
the eggshell by approximately 45–46 times compared to the tradi- and surface hydrophobicity could be due to the unfolding of protein
tional process (submerged in the brine solution, 25% wt/wt, 16 days and then rearrangement of unfolded proteins. At 400 MPa, the emul-
at room temperature) after 48 hr, indicating high level of dehydration sifying activity index was significantly (p < .05) decreased as compared
and salt diffusion (Mai Dang et al., 2014). to the control (untreated) sample. At lower pressures (100 MPa), the
The effect of US treatment (40 W power, 55 C, 5 min) was inves- emulsion stability index was increased, while the decrease was
tigated on Salmonella enteritidis in a liquid whole egg for the inactiva- observed at >200 MPa. Modification of EY at different pressure levels
tion purpose by Huang et al. (2006). A combination of US (40 W might be due to the varying rearrangement extent and aggregation of
power, 55 C) and hydraulic high pressure (138 MPa and 20 C) treat- proteins (Yan et al., 2010).
ments showed a maximum microbial reduction of 3.2-log cycles along Effect of HHP on crosslinking of EW and ovalbumin with trans-
with mild heat (55 C). Furthermore, the combination of two treat- glutaminase to assess the allergenic potential was reported by Ma
ments can be used in place of conventional thermal processing where et al. (2015). Susceptibility of EW and ovalbumin crosslinking to trans-
coagulation of egg proteins, due to high temperature, often causes a glutaminase after HHP treatment (400 MPa, 40 C for 30 min) was
problem (Huang et al., 2006). increased. The high-molecular-weight polymers were created, how-
Overall, the US is capable of changing foaming and structural ever, a significant (p ⩽ .05) amount of unmodified monomeric proteins
properties of EW besides reducing microbial counts. These properties was left in the EW and ovalbumin sample. While the digestibility
could be controlled by changing the US treatment duration, experiments showed that resistance to IgE-binding, immuno-
depending on the end product requirement. Further the reaction rates stimulatory properties, and proteolysis of transglutaminase and HHP
can be shortened when the US is applied to salting process and enzy- treated proteins were not significantly different from those of the nat-
matic hydrolysis as a pretreatment step, which contributes in produc- ural ones, thus do not support the idea of reducing the allergenicity of
ing hydrolysates with improved antioxidant activity and accelerates egg proteins using transglutaminase crosslinking (Ma et al., 2015).
enzyme hydrolysis. In a study, Singh and Ramaswamy (2014) reported the effect of
HHP on antioxidant activity and the degree of hydrolysis of freeze-
dried EW powder and EW protein. HHP can modify the functional
5 | H I G H H Y D R O S T A T I C P R E S S U R E (H H P ) properties of proteins by altering their structure. For instance, HHP
treatment (350–550 MPa for 5–15 min) increases the degree of tryp-
During HHP treatment, the products are placed in a highly special- sin hydrolysis, 2.78 (untreated) to 11.3% in EW protein, and
ized vessel and exposed to a pressure above 100 MPa to maintain 2.20–8.41% in freeze-dried EW powder, at 550 MPa for 15 min, the
food preservation (Yamamoto, 2017). In HPP, no substantial heating degree of hydrolysis was highest. Furthermore, the antioxidant activ-
process is involved therefore, this technology avoids the destruction ity of both (freeze-dried EW powder and EW protein) samples
of valuable food components. However, HHP treatments modify increased (19.0 and 25.00%) after being treated at 350 and 550 MPa
the functional properties by disrupting the hydrophobic regions and for 5 min (Singh & Ramaswamy, 2014).
electrostatic interactions of food components (Marciniak, Suwal, Impact of HHP on hard-cooked peeled eggs (HCEs) (value-added,
Naderi, Pouliot, & Doyen, 2018). Direct HHP application on proteins ready-to-use egg products) as it is susceptible to microbial re-
leads to the modifications in structure depending on the pressure contamination (S. enteritidis) during post-processing stages was evalu-
applied, conditions of solution, protein system and duration and ated by Shahbaz et al. (2018). HHP treatment (500, 550, 600 MPa,
magnitude of pressure treatment, structural modifications occur 5 min, 25 C) was used by researchers as a post-processing terminal
due to the formation of new bonds which further leads to gelation, step to ensure maximum safety of HCEs and its effect of processing
precipitation or aggregation (Khan et al., 2015; Perreault, Hénaux, were evaluated and compared with commercial heat treatment (95 C
Bazinet, & Doyen, 2017). HHP treatment also modifies the interfa- for 40 min). Heat treatment often lead to discoloration in HCEs yolks
cial properties of proteins, which further leads to the alteration of (greenish-gray) but color values after HHP treatment were reported
foaming and emulsifying properties of proteins (De Maria, Ferrari, & to have no significantly different (p > .05) compared to control
Maresca, 2016; Manassero, Beaumal, Vaudagna, Speroni, & (unprocessed HCEs). The thermal and nonthermal treatment kept the
Anton, 2018). growth of microorganism's constant (<104 CFU/g) throughout the
45 days refrigerated storage while in the untreated sample microbial
count exceeds (within 3 days) the safety limit (<104 CFU/g).
6 of 18 AFRAZ ET AL.

TABLE 2 Effect of HPP on egg and egg derivatives

Sample Treatment conditions Overall outcomes References



HCEs 550 MPa, 5 min, 25 C 6.14-log CFU/g reduction in Salmonella. Shahbaz et al. (2018)
enteritidis population
EW 300–600 MPa, 10 min, 20 and Increase lysozyme activity (<6.8 times) Tribst et al. (2018)
50 C at pH 1.5 and improved its stability by
112%
EW 400 MPa pressure, 40 C, for Higher molecular weight polymers, Ma et al. (2015)
30 min unmodified monomeric proteins
EW powder 350–550 MPa pressure, for 8.41% increase in trypsin hydrolysis Singh and Ramaswamy (2014)
5–15 min, 20 C
Liquid whole egg 300 MPa/30 , 2% triethyl citrate, 5-log reduction in Listeria innocua. and Monfort, Ramos, et al. (2012)
52 C/3.50 or 55 C/20 Escherichia coli. population
Egg yolk 100–500 MPa, 10 min, 25 ± 2 C Decreased SH content, decreased Yan et al. (2010)
surface hydrophobicity
EW solutions 400–700 MPa, 10–60 C, Increased turbidity, exposed SH Van der Plancken, Van Loey,
20 min, pH 7.6 and 8.8 content, surface hydrophobicity, and and Hendrickx (2005)
susceptibility to enzymatic hydrolysis
Liquid whole egg 250 MPa, 886 s, 5 C 5-log reduction in Listeria seeligeri Lee, Heinz, and Knorr (2003)
population

Moreover, the HHP post-package pasteurization (550 MPa for 5 min) observed color of the sample was primarily affected by the pressure
showed potential as a non-thermal terminal kill stage for commercial level and the rheological properties (viscosity) were significantly
production of HCEs (Shahbaz et al., 2018). (p < .05) influenced by the length of HPP treatment (Németh
HPP (800 MPa, 5 min, 9–37 C) treatment of EW has been found et al., 2012). The granule fraction of egg yolk (EY) (produced by centri-
to increase its pepsin digestibility to a greater extent than thermal fugation processes) was reported to yield different compositional

treatment (95 C). After HP treatment, pepsin was reported to degrade properties compared to the native yolk, thereby creating opportuni-
the main egg white protein (EWP) (ovalbumin, ovomucin, ties for being used as ingredients in the nutraceutical and food indus-
ovotransferrin, lysozyme) in less than 2 min (Hoppe et al., 2013). Pep- tries. HHP (600 MPa, 5 min) treatment has been used to promote
sin incubation of the pressure-treated EW cause substantial hydrolysis disintegration of the compact structure of EY granule. Upon disinte-
of the majority of proteins and liberate various peptides sequences, gration high concentrations of folate (230 μg/g dry matter) were
which may have bioactivities such as antioxidant activity and ACE released in the plasma fraction of the yolk granule (Naderi, Pouliot,
inhibition. In addition, HP treatment also increase EW digestibility and et al., 2017).
consequently enhance its health benefits (Hoppe et al., 2013). In The combined effect of HHP, heat, and triethyl citrate on a liquid
another study by Savadkoohi et al. (2016), the combined effects of whole egg to design an alternative pasteurization process was evalu-
HP (600 MPa, 15 min, 20 C) and medium (high solid, semi diluted and ated by Monfort, Ramos, et al., 2012, Monfort, Saldaña, et al., 2012.
diluted) concentration on the structure of ovalbumin have shown that HHP treatment applied at 20 C was not sufficient to pasteurize the
it retains the natural conformation in the high solid (80% w/w) liquid whole egg without disturbing its physical properties. Lethality
medium. In an aqueous medium (20% wt/wt), the composition of of treatment was increased when applied at 4 or 50 C. However,
ovalbumin was irreversibly modified and slightly altered in a semi HHP treatment alone may not be enough to declare the liquid whole
dilute (30–60% wt/wt) medium. This change may be due to the fact egg as safe. HHP at 20 or 4 C along with 2% triethyl citrate showed
that ovalbumin is very hydrophobic in nature and HP treatment trig- synergistic lethality and decrease in the resistance of Listeria innocua.
gers rearrangements between disulfide and sulfhydryl bonds and Escherichia. coli (Monfort, Ramos, et al., 2012; Monfort, Saldaña,
(Savadkoohi et al., 2016). et al., 2012). HHP (300 MPa/30 ) at 20 C, 2% triethyl citrate and heat
The use of HHP technology allows the preservation of native treatment at different temperatures (52 C/3.50 or 55 C/20 ), these
qualities of food raw materials with comparable antimicrobial effec- conditions were applied by the researchers. This combined treatment
tiveness to heat treatment, and its beneficial effect has been demon- shown to achieve similar lethality (5-log reduction) of heat ultra-
strated in many heat-sensitive foods. HHP (200–400 MPa, 3–17 min) pasteurization treatment (71 C/1.50 ), in L. innocua and E. coli popula-
treatment has effectively reduced the viable cell count of specific bac- tion of liquid whole egg sample was reported by Monfort, Ramos,
teria (Listeria monocytogenes, S. enteritidis, and Staphylococcus. aureus) et al. (2012), Monfort, Saldaña, et al., 2012. This process retains better
in artificially infected liquid whole egg. The most troublesome bacte- functional, physicochemical properties and certain quality parameters
rium in egg products is S. enteritidis and its reduction was reported compared to ultra-pasteurization treated liquid whole egg (Monfort,
around 2-log CFU/ml (Németh et al., 2012). In addition, the study also Ramos, et al., 2012, Monfort, Saldaña, et al., 2012).
AFRAZ ET AL. 7 of 18

6 | P U L S E D E LE C T R I C FI EL D (P E F ) and flavor of food, and they are influenced by EFs and electromag-
netic waves (Liu et al., 2017; Zhang, Wang, Jiang, & Qian, 2017).
For egg and egg products, PEF is mainly used to destroy microorgan-
isms by employing high-intensity electric fields, further, it retains the
nutritional quality and food flavor (Soliva-Fortuny, Vendrell-Pacheco, 6.1 | Effect of PEF on egg and egg products
Martín-Belloso, & Elez-Martínez, 2017). The working principle of elec-
tric fields (EF) is to modify protein structure that depends upon the Table 3 summarizes the effect of PEF on egg and its derivatives. The
aggregation and unfolding of protein or by generating free radicals impact of PEF and thermal processing on the aggregation of ovomucin
(Barbosa-Cánovas & Zhang, 2019). Different interactions between depleted EW protein solution at varying pH was evaluated by Liu
molecules of protein, comprising Van der Waals forces, disulfide brid- et al. (2017). The heat treatment caused a noticeable protein
ges, hydrophobic and electrostatic interactions, salt bridges, and aggregation in a sample at pH 5, 7, and 9 at 60 C for about 10 min.
H-bonding can be disrupted by free radicals, thus at various dimen- While PEF treatment-induced aggregation at pH 5 and 7, however
sions, functional properties of protein and its structure can be altered at 4 or 9 aggregations did not occur, using constant strength of EF
(Barbosa-Cánovas & Zhang, 2019). Changes in protein structure, also 1.4–1.8 kV/cm besides energy input of 260–700 kJ/kg. Same resul-
influence the properties such as solubility, foaming, apparent viscosity, ts were achieved when samples subjected to varied EF strengths
gelling properties, immunoreactivity, and emulsifying activities, which (0.7–1.7 kV/cm) however the energy input (713 kJ/kg) was kept con-
plays a vital in the food industry (Echeverría, López-Caballero, Gómez- stant. Additionally, samples were more prone to aggregation at pH 5
Guillén, Mauri, & Montero, 2016; Nguyen, Zhang, Barber, Su, & during both PEF and heat treatments. Therefore, PEF has a consider-
He, 2016). Especially solubility properties is the most critical func- able potential to minimize the protein aggregation during processing,
tional properties, which relate to the hydrogen holding and hydro- as EW proteins are heat-sensitive, therefore PEF can be used to retain
philic and hydrophobic surface development on protein structure the ovomucin depleted EW protein in solution which later can be used
(Zhu, Lin, Ramaswamy, Yu, & Zhang, 2017). On the other hand, food in the protein fortification of the drinks (Liu et al., 2017).
allergy is related by immunoreactivity, major public health problem, PEF treatment (25 kV/cm for 400 μs, 1,362.6–2,043.9 kJ/L, 18 C)
and theoretically, a food allergy can be reduced by altering the struc- has not reported to change the colloidal properties of protein solution.
ture of the protein which consequently increase the protein solubility But, when treatment duration increased from 400 to 600 μs, there is
and digestibility (Okolie, Aryee, & Udenigwe, 2018; Zhang, Zhang, an increase in Z-average size (36.9%) and a decrease in insoluble con-
Sheng, Wang, & Fu, 2016). Thus PEF helps to alter the functional tent (7.84%) was observed as compared to control. After PEF treatment
properties and protein structure, the later can influence the quality of protein solution, carbonyl contents were not affected and a slight

TABLE 3 Effect of PEF on egg and egg derivatives

Sample Treatment conditions Overall outcomes References


EW 1.4–1.7 kV/cm field strength, Increased anti-inflammatory and Liu, Oey, Bremer, Carne, and
653–695 kJ/kg energy, 80 C for antioxidant activity, less solution Silcock (2019); Liu, Oey,
10 min turbidity Bremer, Silcock, et al. (2019)
Liquid whole egg 50 kV/cm field strength, 1 Hz pulse >6-log reduction in bacteria Baba et al. (2018)
rate, 10 ml/min flow rate, temp. 4 C
Ovomucin- 1.7 kV/cm, 260–700 kJ/kg, 20 μs pulse Showed similar extent of hydrolysis Liu, Oey, Bremer, Silcock, and
depleted EW width, 50 C, pH 5 and 7 compared to ovomucin depleted EW Carne (2018)
solution heat-treated at 80 C
EW protein 1.4–1.8 kV/cm field strength, Minimized protein aggregation Liu et al. (2017)
260–700 kJ/kg energy, pH 4 or 9,
10 min, 60 C
EW solution 25 kV/cm field strength, for Decreased soluble content, increased in Wu et al. (2014)
400–600 μs, 1,362.6–2,043.9 kJ/L, SH content, and insoluble aggregates
18 C formed
Liquid whole egg 25 kV/cm field strength, 75–100 kJ/kg 9-log reduction in Salmonella . enteritidis Monfort, Saldaña, et al. (2012)
energy, six pulses of 3 μs, 52–60 C population
Liquid egg yolk 45 kV/cm, 419 kJ/kg, 30 μs 4-log reduction in Salmonella Monfort, Gayán, Raso, Condón,
typhimurium and S. aureus 
and Alvarez (2010)
Liquid egg yolk 30 kV/cm field strength, 2 Hz, 2 μs 5-log reduction in S. enteritidis and Amiali, Ngadi, Smith, and
pulse duration, temp. 40 C Escherichia coli. O157:H7 Raghavan (2007)
EW proteins 12.5 kV/cm intensity, 2,465 and Thermostability partially increased, Perez and Pilosof (2004)
1,631 J/ml 10 pulses, 35 C lowered gelation rate
8 of 18 AFRAZ ET AL.

increase in SH contents was reported, which reflects that no oxidation further subjected to heat treatment (55 C for 3.5 min) to kill the resid-
occurred and induced protein unfolding. Moreover, insoluble aggre- ual bacterial population in a liquid whole egg without denaturation of
gates formed after the PEF treatment and their main components were the protein. Such combination reduced S. enteritidis population
ovalbumin, ovotransferrin, and lysozyme (Wu et al., 2014). (p < .05) by 4.3-log reduction and significantly increased the shelf life
The impact of PEF followed by heat treatment in the presence of and caused no changes in color, pH, electrical conductivity, and vis-
triethyl citrate in continuous and static settings in the liquid whole cosity (Hermawan et al., 2004). In another study, the effect of PEF,
egg was studied by Monfort, Saldaña, et al. (2012), as an alternative to temperature, and time to inactivate S. enteritidis and E. coli O157: H7
pasteurization treatment. PEF treatment (25 kV/cm and 75–100 kJ/kg, in liquid EY was investigated by Amiali et al. (2007). Reduction in bac-
6 pulses of 3 μs) followed by heat (60 C/10 , 55 C/20 or 52 C/3.50 ) in terial population was reported in the inoculated (108 CFU/ml) sam-
the presence of triethyl citrate (2%) in liquid whole egg has been ples of EY through E. coli or S. enteritidis. PEF treatment at 20, 30, and
reported by authors to reduce the S. enteritidis population by 9-log. 40 C combined with PEF (intensities 20 and 30 kV/cm 105 pulses
This newly designed treatment/process has been reported to reduce and 2 μs pulse duration, 2 Hz) in a continuous process. Increase in EF
the population of Salmonella serovars enteritidis 4300, Virchow, intensity, heat treatment and processing time caused an increase in
Senftenberg, Dublin, Typhimurium, Tnteritidis 4396 and Typhi by 5-log bacterial inactivation, at about 30 kV/cm EF intensity and heat treat-
reduction in both static and continuous conditions. But, heat pas- ment (40 C), 5-log reduction occurs in S. enteritidis and E. coli. Inacti-
 0  0
teurization treatments (60 C/3.5 and 64 C/2.5 ) reduced 5-log of vation rates of S. enteritidis (0.004–0.098 μs−1) and E. coli
various serovars of Salmonella, only S. enteritidis 4396 and Salmonella (0.009–0.039 μs−1) were increased as the temperature of processing
senftenberg reduced to 3–4 and 2-log, respectively (Monfort, Ramos, amplified from 20 to 40 C, whereas S. enteritidis was way more resil-
et al., 2012; Monfort, Saldaña, et al., 2012). After PEF treatment, it ient than E. coli during PEF inactivation process at lower temperatures
was reported that soluble contents of protein were decreased (5.0, (Amiali et al., 2007).
1.3, and 1.8%) followed by heat treatment (60, 55, and 52 C), The high thermal sensitivity of liquid whole egg components
respectively, in the presence of triethyl citrate additive. While 9.4 limits the production of microbiologically healthy liquid whole egg
and 1.6% of soluble protein content were reduced at 64 and 60 C, with industrial ultra-pasteurization. PEF (25 kV/ and 100 kJ/kg) in
respectively. The authors concluded that newly designed treatment combination with natural essential oils (EO; 200 μl/L of lemon) and
could be used in place of the current heat pasteurization process, as mild heat (60 C) proposes an alternative treatment, which provides a
it showed lethal efficiency against S. serovars with an identical or safety level comparable to ultra-pasteurization, but at a lower temper-
minor reduction in protein soluble contents (Monfort, Ramos, ature. The combined treatment resulted in a 4-log reduction in the
et al., 2012, Monfort, Saldaña, et al., 2012). L. monocytogenes and S. senftenberg 775 W population and when only
The effect of intense PEF (30–50 kV/cm field strength, 1 Hz one of these barriers were used, authors found that the microbial
pulse rate, 10 ml/min flow rate, 4 C) along with mild heat (55 C for inactivation was reduced to 1.5-log of either bacterium (Espina,
2 min), on the liquid whole egg for pasteurization purpose, was inves- 
Monfort, Alvarez, García-Gonzalo, & Pagán, 2014). However, syner-
tigated by Baba et al. (2018). Carboxymethyl cellulose solution with gism was also observed by Espina et al., (2014) in the successive appli-
added lipoproteins from liquid whole egg (CMC+), liquid whole egg cation of PEF, heat and 200 μl/L mandarin, carvacrol, citral, or
(LWE), carboxymethyl cellulose solution (CMC) and lipoprotein limonene EOs. Attaining a 3.5-log reduction in S. senftenberg and
reduced liquid whole egg (LWE−) were used as solvents. Furthermore, 3.0-log in L. monocytogenes. Thus, this combined treatment could be
these liquids were inoculated with Enterobacter aerogenes (107/ml) applied in the food industry to obtain microbiologically safe liquid
and treated with different amplitudes of PEF (30 and 50 kV/cm), ther- whole egg (Espina et al., 2014).
mal treatment below 55 C was employed to increase the lethality of Among the Salmonella serovar, S. enteritidis was reported by
PEF treatment (Baba et al., 2018). A reduced microbial count was Monfort et al. (2010) to be the most resistant strain at the field
achieved after PEF treatment (30 kV/cm) for LWE−, LWE, CMC+, and strength greater than 25 kV/cm during the processing of liquid whole
CMC with 1.6, 1.4, 2.4, and 6.6-log reductions, respectively. When egg. The inactivation level of S. enteritidis was mainly dependent on
PEF was applied at 50 kV/cm, more than 6-log reduction in bacterial the energy being applied such as 106, 272, and 472 kJ/kg for 1, 2,
population for all liquids was observed. Numerical analysis of PEF and 3-log reductions, respectively (Monfort et al., 2010). In another
showed that lipoproteins interfered with the killing effect of bacteria, study it was reported that, polypeptides from EW can be used as
therefore, in contrast to other liquids (which contain more or fewer functional ingredients in food products. PEF technology has been
lipoproteins) bacteria were killed only in CMC solution (Baba used to enhance the antioxidant activity of polypeptides
et al., 2018). (MW 10–30 kDa) from EW proteins. Under specific conditions, PEF
The use of PEF for inactivation of S. enteritidis and shelf life (10 kV/cm, 2000 Hz pulse frequency) showed an increase (28.44%) in
improvement of liquid whole egg was reported by Hermawan, the inhibition of 2,2-diphenyl-1-picrylhydrazyl (DPPH) as compared to
Akdemir Evrendilek, Dantzer, Zhang, and Richter (2004). PEF caused the polypeptide's antioxidant activity, without PEF treatment (Wang
1-log CFU/ml reduction in the population of S. enteritidis, under et al., 2013).
2.12 μs duration of a pulse, the strength of EF 25 kV/cm for 250 μs In another study, effects of PEF at different EF intensities (1.4–
period, in the liquid whole egg sample. The PEF treated sample was 1.7 kV/cm) and energy amplitudes (269–700 kJ/kg, 20 μs pulse width,
AFRAZ ET AL. 9 of 18

50 C) along with heat treatment (60 and 80 C) for about 10 min were and the influence of this treatment on avidin activity was reported by
examined. At different pH environments (pH 4, 5, 7, and 9), the effect Zhu et al. (2018a). They reported a decrease in avidin activity after
of these conditions on antioxidant activity and anti-inflammatory the MW treatment at 60, 70, and 80 C for 1, 3, and 5 min, while the
properties of ovomucin depleted EW was assessed after controlled reduction in activity was greater at 80 C. Furthermore, analysis of
gastrointestinal hydrolysis. An increase in antioxidant activity of secondary structure revealed that an increase in β-sheets occur at
hydrolysates after PEF and heat treatment at pH 4 was reported by 60 and 70 C with an increase in processing time and became constant
Liu, Oey, Bremer, Silcock, et al. (2019), while the anti-inflammatory at 80 C. Whereas α-helices were decreased with time at each temper-
activity of whole hydrolysates was also enhanced after PEF and ature on which MW was applied (Zhu et al., 2018a). The effect of
heating treatment at pH 4. This enhancement was dose-dependent. phosphorylation with MW assistance (200, 300, 400, 500, and
Hydrolysates (1 mg/ml) showed reduction (35.5 and 35.9%) in the 600 W) at pH 8.0 in the presence of sodium tripolyphosphate on
production of interleukin-8 (chemokine) after being treated with PEF structural and foaming properties of EW protein was investigated.
and heat treatment (80 C for 10 min), respectively. PEF processing of Results showed an increase (p-value) in the degree of phosphorylation
ovomucin depleted EW solution can improve the protein hydrolysates at the start of treatment, but it remained constant throughout treat-
with increased anti-inflammatory and antioxidant activity along with ment. Analysis of surface hydrophobicity and spectroscopy revealed
less solution turbidity which can be used in high clarity products and that phosphorylated proteins had a more flexible and unfolded struc-
protein fortified drinks (Liu, Oey, Bremer, Carne, & Silcock, 2019; Liu, ture. Phosphorylated EW protein showed lower content of free SH
Oey, Bremer, Silcock, et al., 2019). groups and higher zeta potential value. After MW treatment (500 W),
foaming stability was increased to 1.1 times, and foaming ability was
increased to 0.44 times as compared to untreated samples, whereas
7 | MICROWAVE TECHNOLOGY (MW) excessive MW treatment (600 W) was reported to decrease the
foaming properties. It was concluded that MW-assisted phosphoryla-
In MW heating, energy transfer in food molecules occurs through tion of EW protein is beneficial to improve its foaming properties
electromagnetic fields (Kalla & Devaraju, 2017) MW treatment, (Li et al., 2018).
energy is supplied by conduction, convection, and radiation due to Singh et al. (2018) investigated the effect of MW
thermal gradients from the surfaces of the material. MW is assumed (10 GHz/22 dBm) radiation for different durations ranging from 2 to
to induce vibration in molecules that lead to cell wall ruptures, leading 60 min on hen EW. They reported that the MW treatment between
to microbial inactivation (Cao, Zhang, Mujumdar, & Wang, 2019). MW 15 and 30 min exposed the buried residues of tryptophan of the
technology due to minimal loss of nutrients, energy efficiency, and native molecule and a higher duration of treatment leads to a compact
food safety has gained popularity, over the last few decades (Pan, structure of the protein, which consequently buried the tryptophan
Sun, Cheng, & Han, 2018; Pu & Sun, 2017; Su, Bakalis, & Sun, 2018). residues again. There was no change in the secondary structure of
The photon energy of MWs is 0.0016 eV at 2.45 GHz whereas, chem- protein even when treated at 60 min as the molecules move back to
ical bond energy is greater than the MW quantum energy therefore their native configuration in 7–8 hr after being removed from the radi-
MW cannot alter the primary structure of a protein (Han, Cai, ation field.
Cheng, & Sun, 2018). However, alteration in tertiary and secondary Furthermore, the outcome of MW pasteurization on the physical
structures can be promoted through MWs with the generation of properties of EW and the whole egg was investigated. Heating unifor-
carbon-centered free radicals (Fan et al., 2016). mity and hot and cold spots during MW pasteurization treatment
were determined. They prepared a sample with the addition of water
in EW and whole egg powder and maintained separate concentration
7.1 | Effect of MW on egg and egg products (30, 27.5, 25, and 20%) of solid, salt contents were 200, 100, 50, and
0 mM. And studied physicochemical properties including water hold-
Table 4 summarizes the effect of MW on egg and its derivatives. The ing capacities, gelation temperatures, dielectric properties, and gel
impact of MW processing on the secondary structure of EW protein strengths. Gelation temperatures of both liquid EW (70 C) and whole

TABLE 4 Effect of MW on egg and egg derivatives

Sample Treatment conditions Overall outcomes References


EW protein 500 W energy, at pH 8.0 Foaming ability and stability increased Li et al. (2018)
EW 10 GHz/22 dBm radiation, for 2–60 Exposed tryptophan residues, no change in Singh et al. (2018)
min secondary structure
EW protein Temp. 60–80 C, for 1–5 min Increased β-sheets, decreased α-helices Zhu et al. (2018a, 2018b)
EW and whole 915 MHz energy, 20–30% solid Water-holding capacity increased, the Zhang, Liu, Nindo, and
egg powder conc., salt content 0–200 mM strength of gel increased Tang (2013)
10 of 18 AFRAZ ET AL.

egg (80 C) samples were in the pasteurization temperature range. The (Ochoa-Velasco, Salcedo-Pedraza, Hernández-Carranza, & Guerrero-
dielectric constants and gelling ability of both types of samples Beltrán, 2018; Pendyala et al., 2020). There are two technologies
decreased with the reduction in solid contents while the treatment which uses UV-C as the source for disinfection, namely Pulsed UV
loss factor was not affected significantly at 915 MHz MW. With the and continuous UV. These technologies use different types of lamps
addition of salt loss factor of samples increased linearly, which as the UV source, and the manner or UV exposure to samples are also
resulted in increased electrical conductivity of samples. MW treated different.
samples showed an increase in water-holding capacity and strength of
gels with an increase in solid concentration, whereas the addition of
salt had no considerable impact on the physicochemical properties of 8.1 | Effect of UV light on egg and egg products
sample (Zhang et al., 2013). Furthermore, functional properties of EW
after in-shell pasteurization by MW heating and by hot water immer- Table 5 summarizes the effect of UV light on the egg and its deriva-
sion were compared by Dev, Orsat, Gariépy, Raghavan, and Ruiz- tives. The efficiency of pulsed UV light and UV-C (254 nm) for the
Feria (2010). Results demonstrated that MW treated in-shell eggs had reduction of enterohemorrhagic E. coli, S. enteritidis, and L. mono-
four times more viscosity, 20% higher enthalpy of denaturation, 30% cytogenes on eggs (shelled) was compared. Bacterial populations
less foam density with 50% more stable foam, and 78% clearer, when were reduced (1.6–3.8-log) when treated with pulsed UV light
compared with water bath pasteurized in-shell EW. MW was proven (1.25–18.0 J/cm2) at different fluences and UV-C light (fluences
a better and viable alternative for the in-shell pasteurization and 0.05–3.0 J/cm2) for 5–300 s. Treatment with UV-C light achieved a
heating of eggshells (Dev et al., 2010). higher reduction (3.2-log at 2 mW/cm2 for 25 s) in bacterial cells at
lower fluences. On the other hand, when bacterial load shielded in
feces or stacked on a small area, pulsed UV light gave higher bacterial
8 | ULTRAVIOLET (UV) LIGHT reduction (1.3–2.2-log) due to its higher penetration power as com-
pared to UV-C light. After UV light treatment, the integrity of the egg-
The UV light (UV-C) has germicidal properties as it produces non- shell was maintained while slight sensory deviations were highlighted
ionizing radiation at wavelengths in the range of 200–280 nm, there- by the panelists after treated with higher doses. Researchers con-
fore it can be used for surface decontamination for fluid foods and cluded that pulsed UV and UV-C light treatments might be useful for

ingredients (Gayán, Serrano, Alvarez, & Condón, 2016). The effective- the decontamination of egg surfaces and overcome the hazard of sal-
ness of UV technology as a disinfectant is well known for over six monellosis infections in humans (Holck et al., 2018). Moreover, the
decades (Pendyala, Patras, Ravi, Gopisetty, & Sasges, 2020). Types of influence of UV light (10.6 and 63.7 kJ m−2, 35.4 W/m2, 5, and
UV is based on the wavelength; UV-A between 315 and 400 nm 30 min) on certain properties (particle size, free SH contents, protein
(longwave), UV-B from 280 to 315 nm (medium wave) and UV-C fractions, absorbance, gelling, foaming properties, immunoreactivity
between 200 and 280 nm (Lante, Tinello, & Nicoletto, 2016; Tremarin, and viscosity) of EW was investigated. Large protein aggregate was
Brand~ao, & Silva, 2017). As most microorganisms absorb ultraviolet formed due to change in SH contents, protein backbone cleavage, and
light at 254 nm, UV-C is the UV of interest in food processing due to development of browning as a result of UV exposure, whereas EW
its germicidal effects. UV-C alters the microbial cell's DNA which proteins were sensitive to UV processing. There was no change in gel
inhibits them from further replication by forming two thymines firmness, immunoreactivity, and gelling temperature, while UV light
next to each other in DNA chains during the UV treatment treated EW produced higher stability foams. The latter effect was

TABLE 5 Effect of UV on egg and egg derivatives

Sample Treatment conditions Results References


2
Whole egg Pulsed UV 1.25–18.0 J/cm , UV-C 1.6–3.8-log reduction in microbes Holck, Liland, Dromtorp, Carlehog,
(surface treatment) 0.05–3.0 J/cm2, 2 mW/cm2, 5–300 s and Mc (2018)
Liquid egg (inoculated 0.75 × 103 J/m2, sample thickness 1, 2, Reduction in microbial population Mehdizadeh, Minaei, Torshizi, and
with salmonella) and 3 mm, 3–15 min, stored at Mohajerani (2015)
5–37 C for up to 8 days
EW 10.6 and 63.7 kJ/m, 35.4 W/m2, 5 and Larger protein aggregate, browning Manzocco et al. (2012)
30 min
Liquid EW 9.22 J/cm2, 3.94 mW/cm2 for 39 min 5.3-log reduction in Salmonella . De Souza and Fernández (2011)
enteritidis
Eggshells 23.6 ± 0.1 J/cm2 dose, for 20 s, 9.5 cm 5.3-log CFU/cm2 reduction in S. Keklik, Demirci, Patterson, and
below UV lamp enteritidis Puri (2010)
Liquid EW 44 J/mL, 50 C, 160 s, 330 ml/min flow 4.3-log reduction in Escherichia coli. Geveke (2008)
rate
AFRAZ ET AL. 11 of 18

attributed to protein aggregate, which filled empty spaces in between egg, and EY) was determined. Results described that nutrients in eggs
bubbles and might be because of the increased viscosity of the aque- were fairly stable to the UV-C light treatment except for carotenoids
ous phase and higher viscosity was also related to increased foam vol- (61% loss), ascorbic acid (66% losses), and retinol (80% losses). UV-C
ume (Manzocco et al., 2012). treated egg fractions showed improvement in foaming ability and its
Effect of UV radiation (0.75 × 103 J/m2) on the thickness, func- stability and 20% increment in the emulsifying activity index as com-
tional properties (foaming ability and stability), storability, and bacte- pared to the pasteurized samples. It was revealed that UV processing
rial activity of liquid egg was investigated. A reduction in the not only sustains most of the nutritive properties of an egg but also
population of Salmonella was consistent in egg samples, while maintain or even increase the functional properties of egg and egg
improvement in functional properties and protein oxidation was also products (Poliana Mendes De Souza et al., 2015). Furthermore,
obtained. When treated at 5 C, a decrease in protein oxidation and (Geveke, 2008) investigated the effect of UV light (44 J/ml) on liquid
Salmonella population was observed after 2 days of storage. UV irradi- EW to compare its efficiency with conventional pasteurization
ation can be used to reduce the microbial population but not below method, which damages the functional properties of the egg. EW
the safe level in a liquid egg. A UV treatment duration of 5 and 10 min sample was injected with E. coli and passed through the UV system at
were considered to be the best for stability and foaming ability, a specific flow rate of 330 ml/min. The effect of temperature
respectively (Mehdizadeh et al., 2014). (30–50 C), pH (7–9), and treatment time (0–160 s) on the inactivation
Toxicological and microbiological contaminants are of vital signifi- of E. coli in EW samples was studied. 4.3-log reduction in the popula-
cance because of their impact on human life and diseases caused by tion of E. coli was reported during its exposure to UV treatment at
raw food materials which directly or indirectly contaminate other food- 50 C for 160 s, this reduction was linearly based on the treatment
stuffs, perhaps the most prevalent health concern in the world today. time. Furthermore, the inactivation of E. coli was inversely dependent
Effect of UV (254 nm, 3–15 min) irradiation conditions, sample thick- on pH in the EW sample and directly dependent on temperature.
ness (1–3 mm) and temperature (3–15 C) of storage on functional
properties, storability and bacterial activity of liquid egg (separated yolk
and albumen), with Salmonella suspension spiked (108/ml), was investi- 9 | COLD PLASMA (CP)
gated. The total viable count of Salmonella reduced in all samples, but
not to the safe level (<2-log CFU/g). The best irradiation times were CP technology has been viewed as beneficial for the inactivation of
10 and 5 min for the purpose of to improving foam strength and stabil- microbes while maintaining the quality of fresh produce (Liao
ity, respectively. However, after 2 days of storage, protein oxidation et al., 2017). On the other hand, this technique is not effective in food
and total Salmonella count were only decreased in the 5 C treatment systems of a controlled environment for the inactivation of enzymes or
of liquid egg sample (Mehdizadeh et al., 2014). UV (253.7 nm, 30 W for microbes, as they are present in intact tissues and CP technology is a
30–120 min) irradiation has also been reported to improve the emulsi- surface phenomenon. CP technology can be used to prevent browning
fying and functional properties of EW proteins by inducing cross- by inactivation of endogenous enzymes (polyphenol oxidase and peroxi-
linking. Thus, EW could be used as a novel foaming and emulsifying dases) (Kang, Roh, & Min, 2019; Misra, Pankaj, Segat, & Ishikawa, 2016).
agent in a wide variety of food systems (Kuan, Bhat, & Karim, 2011). It is considered as a modern technique for the modification of starch
Effect of UV-C radiation on decontamination efficiency (such as S. and altering its chemical and physical properties. CP is an eco-friendly
enterica subsp. enterica Ser. Enteritidis) and quality attributes of liquid process and used for the preservation of food items as an alternative to
egg products was investigated. In contrast to heat treatment, pH and common techniques (Bourke, Ziuzina, Boehm, Cullen, & Keener, 2018).
viscosity were not affected by UV-C treatment while slight browning The inactivation effect of CP is caused by DNA modification and
observed because of the Maillard reaction that occurred in the whole improper replication of cells (Georgescu et al., 2017).
egg and EY at low UV-C doses. Despite that, browning was not as
severe as the conventionally pasteurized egg fractions. The change was
attributed to the lipid oxidation. TBARS values during maximum UV-C 9.1 | Effect of CP on egg and egg products
doses were greater than in pasteurized whole egg and EY, while results
did not differ considerably as compared to the untreated samples. Table 6 summarizes the effect of CP on egg and its derivatives. The
UV-C treatment effectively inactivate the S. enteritidis population, in EY effect of novel CP on the eggshell surface for the inactivation of
and whole egg up to 3.3-log and 3.8-log, while 5.3-log-reduction was S. enterica serovar Enteritidis was investigated. Eggshells were contam-
achieved in EW under dynamic conditions (9.22 J cm−2, 39 min). Static inated (107 CFU/egg) with S. enteritidis and then treated with atmo-
treatments although proved to be less effective but still reduced the spheric pressure plasma (APP) with different experimental settings,
load of bacterial cells between 1.7 and 2.8-log reduction. Further, it rate of gas flow ranges from 2000 to 3,000 L/h, exposure times
was revealed that duration requires to achieve a 4D reduction of Sal- (60–120 s), plasma jet distance ranges (15 or 40 mm), reference volt-
monella cells, at 3.94 mW/cm2 was around 7.4 min in EW (de Souza & ages (100–80%), and frequencies (20–25 kHz). The reported reduc-
Fernández, 2011). tion (<102 CFU/egg) was lower than the detection limit, in the
The impact of UV-C light on minerals, key secondary metabolites concentration of S. enteritidis on egg surface at an extreme plasma
such as zeaxanthin, lutein, and vitamins of egg segments (EW, whole power of 655 W for 120 s of treatment. There was not any negative
12 of 18 AFRAZ ET AL.

TABLE 6 Effect of CP on egg and egg derivatives

Sample Treatment conditions Results References


Eggshell (inoculated with 655 W (25 kHz–100% V), for 120 s Reduction in S. enteritidis below Dasan
Salmonella. enteritidis) the detection limit (102 CFU/egg) et al. (2018)
Egg (surface 10–12 kHz frequency, 25–30 kV voltage, Reduction in salmonella population, Georgescu
He/O2 for indirect treatment, for 10 below the detection limit (102 CFU/egg) et al. (2017)
and 25 min
Eggshell (inoculated with S. enteritidis) 85 kV voltage, for 15 min 5.53-log CFU/egg reduction on surfaces Wan et al. (2017)
Eggshell (inoculated with S. aureus) 21 kHz frequency, 1 kV voltage, 1.8–2.5-log reduction in S. aureus, and Dobeic
for 10–60 s native aerobic mesophilic bacteria et al. (2016)
Eggshell (inoculated with RH 35 and 65%, at 25 C, for 90 min 2.5–4.5-log CFU/eggshell reduction Ragni
S. enteritidis and S. typhimurium) et al. (2010)
Eggshell Air, 21–23 C for 90 min 4-log reduction in Enteritidis MB2509 Vannini
population et al. (2009)

effect on egg quality because temperature stayed below 35 C during observed. There was no significant difference in the quality attributes
the treatments (Dasan et al., 2018). Moreover, the effect of CP on egg of eggs treated under direct and indirect methods (Wan et al., 2017).
surface for the inactivation of S. enterica either with direct treatment S. typhimurium poses a serious hazard to the safety of poultry eggs by
(eggs dipped in plasma) or indirect treatment (eggs outside the plasma forming biofilms on eggshells. Cold nitrogen plasma (CNP) technology
zone) was studied. They used 25–30 kV voltage and 10–12 kHz fre- has an inhibitory effect on the forming of such biofilms. After CNP
quency and eggs were polluted with Salmonella population (108). (600 W, 2 min) treatment the metabolic activity of S. typhimurium
He/O2 compound was used to perform direct treatment while in indi- reduced by 82.2%. The mechanism involves: CNP produces hydroxyl
rect treatment air was used as working gas. Reduction in Salmonella radicals (by reaction with water) which consequently trigger an
population (<102 CFU/egg) was below the detection limit, after the increase in the intracellular oxidative stress. The extracellular polysac-
direct treatment of 10 min and indirect treatment of 25 min, with a charide (32.1–8.4 μg/ml), protein (68.5–12.3 μg/ml) and extracellular
relative humidity of 80% as the experiment confirmed the importance DNA (26.5–8.6 μg/ml) were also decreased as a result of CNP treat-
of humidity in the inactivation process (Georgescu et al., 2017). ment (Lin, Liao, Li, Abdel-Samie, & Cui, 2020).
The potential of atmospheric CP for the external decontamination
of eggs in the shell was studied as in European Union, eggs may not
be washed or cleaned. A reduction of 1.8–2.5-log in S. aureus and 10 | R A D I O F R E Q U E N C Y ( RF )
native aerobic mesophilic bacteria on eggshells after 10–60 s of treat-
ment was reported by Ragni et al. (2010). Plasma treated eggs were RF and MW both are nonionizing forms of electromagnetic energy
not significantly different from the untreated eggs for 54 days in the and RF has a longer wavelength (Han et al., 2018). This technique has
case of physicochemical properties. The treatment of eggshells with been widely studied as it overcomes the traditional heating methods
plasma jet has no side effect on egg quality and has the potential for because of their low heating rate, RF heat volumetrically instead of
the decontamination (Dobeic et al., 2016). Furthermore, the decon- surface heating (Guo, Mujumdar, & Zhang, 2019). In recent studies,
tamination power of gas plasma on eggshell samples was evaluated the application of RF energy in food processing was evaluated includ-
which were artificially inoculated with S. enteritidis (5.5-log CFU/egg) ing blanching, pasteurization, drying, heating of bread, and thawing
and S. typhimurium (6.5-log CFU/egg). Different experimental condi- (Zhao, Zhao, Yang, Singh Sidhu, & Kong, 2017). RF heating was con-
tions were considered such as, relative humidity in the chamber (35% sidered as an alternative to conventional heating such as for disinfec-
and 65%, at 25 C), and decontamination times (10, 20, 30, 45, 60, and tion, cooking, blanching, thawing and also for the treatment of fresh
90 min) at room temperature. A reduction of 2.5 and 4.5-log foods (Guo et al., 2019; Hou, Johnson, & Wang, 2016; Zhang, Lyng, &
CFU/eggshell was reported in the population of S. enteritidis using low Brunton, 2004; Zhang et al., 2017; Zhang, Chen, Mujumdar, Zhong, &
and high humidity, respectively. While there were no significant nega- Sun, 2015). In response to RF fields, cell death occurs as a result of
tive effects on the quality of eggs, and 90 min treatment is feasible frictional interaction between polarized molecules and charged ions
for industries and farmers who stock eggs longer than that is neces- (Kou, Li, Hou, Zhang, & Wang, 2018).
sary for sterilization (Ragni et al., 2010).
CP (85 kV, 5–15 min) were used for the inactivation of Salmonella
from spot inoculated eggshells under different modes of exposure, in 10.1 | Effect of RF on egg and egg products
dry air (direct) and modified atmospheric gas (MAG) environment
(indirect). Inactivation of Salmonella was reported to be dependent on Table 7 summarizes the effect of RF on egg and its derivatives.
the mode of exposure, gas type, and treatment time. Eggshells directly Boreddy et al. (2014) evaluated the impact of RF assisted thermal
treated under MAG for 15 min a reduction of 5.53-log CFU/egg was treatment on EW powder was evaluated to retain the functional
AFRAZ ET AL. 13 of 18

TABLE 7 Effect of RF on egg and egg derivatives

Sample Treatment conditions Results References



Eggshell 40.68 MHz RF, 30–45 W, 30–38 C, >5-log reduction in salmonella Yang et al. (2019)
2.5–8 min, population
Egg yolk (inoculated 60 MHz RF energy, 35.0 and 6.5-log reduction in the population of E. Geveke et al. (2017)
with Escherichia coli.) 56.7 C, 23.5 min coli
EW powder 6 kW, 27.12 MHz RF energy, 90 C Pasteurization and improved the gelling Boreddy et al., 2016)
for ≥8 hr properties
EW powder 90 C, holding at 8 hr or longer Better functional properties, ≥7-log (Boreddy et al. (2014)
reduction in Salmonella spp.
EW and egg yolk 10 MHz to 3 GHz, 5–56 C, 30 min Increased coagulation and turbidity, Kannan, Dev, Gariépy, and
decreased foam stability and viscosity Raghavan (2013)

properties, energy requirements, and decreasing storage time in a hot heated additionally for 20 min at 56.7 C. They reported a 6.5-log

room. EW powder stored in an elevated temperature (58–60 C) reduction in E. coli's population with this two-step process, while the
chamber for 10–14 days traditionally while EW protein (pH  9.5) total time for the process was 23.5 min, whereas in conventional
was heated via RF at various temperatures (60–90 C), and then stored method 60 min of processing is required for 6.6-log reduction of

at the same temperature for 60 min, which exceeds 3 days at 60 C. It E. coli using just hot water. The authors concluded that this novel pas-
was reported that 90 C treatment followed by storage time of teurization process was significantly faster than the conventional/
8–24 hr, in hot air oven, provides optimum functional properties. RF commercial process (Geveke et al., 2017).
assisted thermal processing on all the above-discussed parameters did Additionally, the effect of treatment time, RF power, and temper-
not reduce the solubility, moisture content, and color lightness signifi- ature of cooling water on S. typhimurium inactivation in shell eggs and
cantly when compared to the traditionally processed samples, but interior quality were evaluated. They used different processing param-
foaming capacity was significantly lower than the traditionally eters such as RF; 40.68 MHz; power 30–45 W; treatment time
processed sample. It was also reported that the foaming stability, gel 2.5–8 min and temperature 30–38 C, compared with hot water treat-
firmness, gel elasticity, and water-holding capacity was similar to RF ment at 56.7 C for 15 min. The >5-log reduction in Salmonella popula-

assisted treatment at 90 C followed by holding for 8 hr or longer in a tion was reported after employing the above-mentioned conditions
hot air oven. It was concluded that 90 C treatment and holding time without significant quality changes. It was further revealed that the
of 8 hr or longer in a hot air oven produced parallel or to some extent shortest (35 W power for 4.5 min at 38 C) and the longest (30 W for
better functional properties as compared to the conventionally 8 min at 30 C) combined treatments considerably (p < .05) preserved
processed EW protein. These conditions also achieved a ≥ 7-log the quality better as compared to the commercial hot water pasteuri-
reduction in Salmonella spp. Therefore, it could be used to shrink the zation (56.7 C for 60 min). There is no significant (p ≥ .05) change in
pasteurization time from the existing 10–14 days to <24 hr. the quality of egg between the shortest and longest treatment except
Moreover, the impact of RF heating on egg dielectric (polarized) for the shortest duration treatment resulted in greater albumin activ-
properties was studied by Kannan, Dev, Gariép, and Vijaya ity. So, the industry may go for the shortest RF treatment because the
Raghavan (2013). At different temperatures from 5 to 56 C and fre- longest treatment consumed 78% more time and 47% more energy as
quency from 10 to 3 GHz to devise a heating standard wherein there compared to the shortest treatment (Yang et al., 2019).
is minimal unfavorable effect to the egg components (EW and yolk).
They determined heating process parameters, based on a dielectric
study. Dielectric properties of EW closely resemble with water 11 | A D V A N T A G E S A N D D I S A D V A N T A G E S
because of its increased water content. While eggshell and shell mem- OF USING N O V EL PROCES SING
brane in their dielectric properties showed great transparency to radio T E C H N O L O G I E S F O R E G G P RO D U C T S
waves thereby paving the way of in-shell egg pasteurization by RF
heating. After RF treatment, an increase in coagulation and turbidity, Novel processing technologies have been reported to significantly
and a decrease in foam stability were reported as compared to the improve the techno-functional properties of different egg products
control sample (Kannan et al., 2013). and increase their usage spectrum in food industry. Non-thermal
A two-step process that uses hot water and RF energy were novel techniques aid in the processing of heat sensitive egg products
developed by (Geveke et al., 2017), to pasteurize the eggs in half time and maintain its natural sensory properties. Under severe conditions
as compared to the commercial hot water process that required about required to achieve microbial safety of egg products, non-thermal
60 min to complete. The sample (EY) was injected (7.5-log CFU/ml) processing technologies could deteriorate the quality of the egg prod-
with E. coli, then heated for 3.5 min at 35 C via 60 MHz RF energy, uct, including color, viscosity, and oxidation of lipids/proteins. Con-
which preferentially heated to 61 C. Secondly, the sample was further cerning viscosity, HHP processing-induced 20% increase in the
14 of 18 AFRAZ ET AL.

viscosity of the liquid whole egg will make the product unacceptable AUTHOR CONTRIBU TIONS
as an indirect protein denaturation or coagulation index would act as Muhammad Talha Afraz: Conceptualization; writing-original draft.
an increase in viscosity. Since proteins are prone to pressure or heat Moazzam Rafiq Khan: Conceptualization; validation; writing-review
variations in liquid egg products, processing-induced high viscosity and editing. Ume Roobab: Writing-original draft; writing-review and
increases the probability of deteriorating protein functionality such as editing. Noranizan Mohd Adzahan: Visualization; writing-review and
foaming or emulsification (Monfort, Ramos, et al., 2012; Monfort, editing. Brijesh K. Tiwari: Conceptualization; writing-review and
Saldaña, et al., 2012). It has been reported that HHP processing editing. Muhammad Inam-ur-Raheem: Supervision; writing-review
improves the viscosity of yolk, EW, and whole egg, but higher pres- and editing. IV.Muhammad Tayyab Rashid: Validation; writing-review
sures and longer periods of pressure usually negatively affected the and editing. Seyed Mohammad Bagher Hashemi: Writing-review and
viscosity (Ramaswamy, Singh, & Sharma, 2015; Singh, Sharma, & editing. Rana Aadil: Conceptualization; supervision; writing-original
Ramaswamy, 2015). draft; writing-review and editing.
PEF processing applied (intensity-dependent manner) to liquid
whole egg caused a minor but not significant increase in viscosity.
OR CID
After PEF processing, pre-homogenized liquid whole egg retained the
Ume Roobab https://orcid.org/0000-0002-6075-6737
same viscosity (Liu, Oey, Bremer, Carne, & Silcock, 2019; Liu, Oey,
Seyed Mohammad Bagher Hashemi https://orcid.org/0000-0002-
Bremer, Silcock, et al., 2019). The type of product determines the
3420-0057
effect of ionizing radiation on the viscosity of egg and egg products
Rana Muhammad Aadil https://orcid.org/0000-0002-0185-0096
being processed. Liquid EW subjected to irradiation demonstrated a
decrease in viscosity with an increased dose of irradiation. Neverthe-
RE FE RE NCE S
less, after irradiation, the viscosity of liquid EY (separated from irradi-
Aadil, R. M., Khalil, A. A., Rehman, A., Khalid, A., Inam-ur-Raheem, M.,
ated shell eggs) or an irradiated whole egg powder solution increased
Karim, A., … Afraz, M. T. (2020). Assessing the impact of ultra-
(Liu, Oey, Bremer, Carne, & Silcock, 2019; Liu, Oey, Bremer, Silcock, sonication and thermo-ultrasound on antioxidant indices and polyphe-
et al., 2019; Min, Nam, Jo, & Ahn, 2012). In order to reap the benefits nolic profile of apple-grape juice blend. Journal of Food Processing and
offered by these technologies, it is crucial to identify the boundaries Preservation, 44(5), e14406. https://doi.org/10.1111/jfpp.14406
Aadil, R. M., Zeng, X. A., Han, Z., Sahar, A., Khalil, A. A., Rahman, U. U., …
of treatment conditions that would work to the advantage of the
Mehmood, T. (2018). Combined effects of pulsed electric field and
intended processing objectives and vice versa. ultrasound on bioactive compounds and microbial quality of grapefruit
juice. Journal of Food Processing and Preservation, 42(2), e13507.
https://doi.org/10.1111/jfpp.13507
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12 | CONCLUSION AND FUTURE
tic effect of temperature and pulsed electric field on inactivation of
PERSPECTIVES Escherichia coli O157:H7 and Salmonella enteritidis in liquid egg yolk.
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